A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332212



Internal ID20865381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16849201..16973400hg38UCSC Ensembl
chr1:17175696..17299895hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38124200
hg19124200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv100n223
Supporting Variantsnssv18201540
Samples
Known GenesCROCC, MIR3675
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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